ConductScience.org, home

Comparison · NCT00866697-sae

Pazopanib vs Placebo: serious adverse events

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

Download JSON
Cite this record

ConductScience Library. Pazopanib vs Placebo: serious adverse events. Trial comparisons, record NCT00866697-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00866697-sae

On this page

Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.2540.2170.295wilson
Risk in group 20.1110.08520.143wilson
Risk difference, group 1 minus group 20.1430.09420.191newcombe hybrid score
Risk ratio, group 1 over group 22.291.73.1log
Odds ratio, group 1 over group 22.731.913.9log
Number needed to harm, for one more participant with a serious adverse event on Pazopanib than on Placebo6.995.2310.6from the risk difference interval

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1PazopanibPazopanib121477EG001
Group 2PlaceboParticipants received matching placebo once daily for a maximum of 24 months.51461EG000

Harm

What it counts
Total, serious adverse events
Time frame
Adverse events were reported from first dose of study treatment until end of study treatment plus 28 days post treatment, up to a maximum duration of approximately 25 months.

Source ClinicalTrials.gov

Trial

Title
Efficacy and Safety of Pazopanib Monotherapy After First Line Chemotherapy in Ovarian, Fallopian Tube, or Primary Peritoneal Cancer
NCT number
NCT00866697
Phases
PHASE3
Conditions
Ovarian Cancer
Interventions
Pazopanib, Placebo
Lead sponsor
Novartis Pharmaceuticals
Results first posted
2013-12-19

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

For software

Read this comparison from software.

The record is JSON. No key.

GET https://conductscience.org/api/comparisons/v1/NCT00866697-sae